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Molecular genetic factors influencing outcomes of Helicobacter pylori infection at Khakasia republic inhabitants

Abstract

Aim of investigation. To detect molecular-genetic features of Helicobacter pylori and polymorphism of main immunoregulatory interleukins genes at Khakases, to estimate their effect on outcomes of infection pathogen.

Material and methods. Investigation was carried out at native population of Khakasia with H. pyloriassociated diseases: peptic ulcer and chronic gastritis. Prevalence of interleukins IL1β, IL1Ra, IL8 and CYP2C19 gene polymorphism was studied by restriction analysis, VacA +– and CagA +– subtypes of H. pylori – by polymerase chain reaction.

Results. Peptic ulcer was associated to S1S2 Vac A subtypes at Caucasians, while at Khakases – to Cag А strains of H. pylori. Interrelation between CagA, АА251 ILs – 8 and the risk of peptic ulcer development was revealed at Khakases (OR=3,1, 95% CI 1,1–8,8). Most common variants among Khakases were – СС +3953 IL1 β (84%) and R4/R4 IL1Ra (76%), with not high expression level. Frequent genotype wt/wt +681 CYP2C19 (89,3%) was associated to the risk of peptic ulcer development (OR=4,17, 95% CI 1,04–19,39).

Conclusions. Population-based genetic determinants (СС +3954 IL1β, R4/R4 IL1Ra), that establish higher protection level from H. pylori-associated diseases at Khakases, than at Caucasians were revealed. Risk factors for peptic ulcer at Khakases include carriage of CagA H. pylori strain, АА-251 of IL8 gene, GG +681 of CYP2C19 gene.

About the Authors

Ye. S. Ageyeva

Russian Federation


O. V. Shtygasheva

Russian Federation


N. V. Ryazantseva

Russian Federation


V. V. Tsukanov

Russian Federation


References

1. Кононов А.В. Воспаление как основа Helicobacter pylori-ассоциированных болезней // Арх. патол. – 2006. – Т. 68, вып. 5. – С. 3–10.

2. Штыгашева О.В., Цуканов В.В. Ассоциация саg A и vac A штаммов Helicobacter pylori и язвенной болезни в организованной популяции г. Абакана // Рос. журн. гастроэнтерол. гепатол. колопроктол. – 2004. – Т. 14, № 2. – С. 84–87.

3. Bamford K.B. Gastric T cell and H. pylori: regulation of pathogenesis and prevention // The immunobiology of H. pylori: from pathogenesis to prevention / Eds. P.B. Ernst, P. Michetti, P.D. Smith. – New York–Philadelphia: Lippincott-Raven Publishers, 1997. – P. 227–236.

4. Blaser M. Ecology of Helicobacter pylori in human stomach // J. Clin. Invest. – 1997. – Vol. 100. – P. 759– 762.

5. Campbell D.I., Warren B.F., Thomas J.E. The African enigma: low prevalence of gastric atrophy, high prevalence of chronic inflammation in West African adults and children // Helicobacter. – 2001. – Vol. 6, N 4. – P. 263–267.

6. Everhart J.E. Recent developments in the epidemiology of Helicobacter pylori // Gastroenterol. Clin. North Am. – 2000. – Vol. 29, N 23. – P. 559–578.

7. Goodwin C.D. Duodenal ulcer, Campylobacter pylori and the «leaking roof» concept // Lancet. – 1988. – Vol. 2, N 8626/8627. – P. 1467–1469.

8. Keates S., Keates A.C., Warny M. et al. Differential activation of mitogen-activated protein kinases in AGS gastric epithelial cells by cag+ and cag– Helicobacter pylori // J. Immunol. – 1999. – Vol. 163. – P. 5552– 5559.

9. Lanas A., Hirschowitz B.I. Influence of smoking on basal and on vagally and maximally stimulated gastric acid and pepsin secretion // Scand. J. Gastroenterol. – 1992. – Vol. 27, N 3. – P. 208–212.

10. Miwa H.H., Go M.F., Sato N. Pylori and gastric cancer: the Asian enigma // Am. J. Gastroenterol. – 2002. – Vol. 97, N 5. – P. 1106–1112.

11. Moran A.P. The role of lipopolysacchande in Helicobacter pylori pathogenesis // Aliment. Pharmacol. Ther. – 1996. – Vol. 10. – P. 57–64.

12. Peek R.M., Moss S.F., Tham K.T. et al. Helicobacter pylori cagA+ strains and dissociation of gastric epithelial cell proliferation from apoptosis // J. Natl. Cancer Inst. – 1997. – Vol. 89, N 12. – P. 863–868.

13. Perez-Perez G.I., Olivares A.Z., Foo F.Y. et al. Seroprevalence of Helicobacter pylori in New York City populations originating in East Asia // J. Urban Health. – 2005. – Vol. 82. – P. 510–515.

14. Rieder G., Einsiedl W., Hatz R.A. et al. Comparison of CXC chemokines ENA-78 and interleukin-8 expression in Helicobacter pylori-associated gastritis // Infect. Immun. – 2001. – Vol. 69. – P. 81–88.

15. Sato Y., Sugamura K., Mochizuki T. et al. Regional differences on production of chemokines in gastric mucosa between Helicobacter pylori-positive duodenal ulcer and gastric ulcer // Dig. Dis. Sci. – 1999. – Vol. 44. – P. 2390–2396.


Review

For citations:


Ageyeva Ye.S., Shtygasheva O.V., Ryazantseva N.V., Tsukanov V.V. Molecular genetic factors influencing outcomes of Helicobacter pylori infection at Khakasia republic inhabitants. Russian Journal of Gastroenterology, Hepatology, Coloproctology. 2010;20(4):16-21. (In Russ.)

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